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The Gymboree Corp., of San Francisco, Calif.

The Gymboree Corp., of San Francisco, Calif. Recalls

All product recalls associated with The Gymboree Corp., of San Francisco, Calif..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 35201–35220 of 37665 recalls

Caroline Flower Baby Sandals (Gymboree) – Size Safety Concern (2005)

Choking Hazard

This recall includes the Caroline Flower Baby Sandal with SKU number 140002069 sold in sizes 1 to 8. The SKU number is printed on the price tag above the bar code. The sandal has a white upper sole and a cork covered outer sole. A white decorative plastic flower is attached to the top of the front strap. The front and back strap have adjustable touch fasteners. The name "Gymboree" is printed in aqua on the sole of the sandal.

CPSCAug 12, 2005Nationwide• The Gymboree Corp., of San Francisco, Calif.

Event Medical: INSPIRATION Ventilator Model Numbers: F7100000-XX, F7200...

Firm received reports of combustion within the blender system of the Inspiration Ventilator.

FDAAug 12, 2005Nationwide• Event Medical

Stryker Howmedica Osteonics Corp.: T2 Recon Nail System.

The blister pack containing the Recon 6.5 Lag Screws may become damage during shipment resulting in loss of sterility.

1...1759 176017611762 1763...1884

Page 1761 of 1884Next

FDAAug 12, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Holmes® Tower Heater Fans (Holmes Group) – Electrical Safety (2005)

Fire/Burn Risk

The recall involves Holmes® models HFH6498-U, HFH6500-U and HFH6500TG-U and Bionaire® model BFH3530-U. The recalled heaters also have date codes beginning with 2604 through 3804 for all units, except for Holmes® model 6500TG-U, which has date codes ranging from 2604 through 4704. The model and date code can be found on the silver label on the back of the unit. The heater fans are 26 inches tall; come in all gray, two-tone gray, or black and gray; and have either the word Holmes® or Bionaire® printed on the front of the base.

CPSCAug 11, 2005Nationwide• The Holmes Group Inc., of Milford, Mass.

Stryker Howmedica Osteonics Corp.: Scorpio Total Knee Cruciate Retaining Femoral Component, ...

The Left Scorpio Total Knee Cruciate Retaining Waffle Femoral Component #7 packaged and labeled as left may contain a Right and vice versa.

FDAAug 11, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Ritchey Bicycle Wheels (Ritchey Design) – Rear Wheel Issue (2005)

The above wheels were sold by Ritchey as wheel sets and as rear wheel only and as original equipment on 2004 model year Fuji and Motobecane USA bicycles and the 2005 model year Prestige road bike from Raleigh. The recalled wheels have high flange hubs measuring 60 milimeters in diameter and the hub body is straight between the flanges.

CPSCAug 11, 2005Nationwide• Ritchey Design, of San Carlos, Calif. (manufactured under license from American Classic Inc., of Tampa, Fla.)

Boston Scientific Corporation One Boston: Renegade Hi-Flo Microcatheter Kits, Catalog/Order # 18-29...

Outer box of the product may have an incorrect expiration date listed as 2007-06, while the correct expiration date is 2007-04

FDAAug 10, 2005KY, TX• Boston Scientific Corporation One Boston

Kelty Speedster Jogging Strollers (Kelty) – Frame Safety Concern (2005)

The recalled strollers have an aluminum frame and a cloth seat with a sun canopy. The recalled single seat Speedster Deluxe stroller has model number 20050116 and serial numbers: S2000001D0504 through S2000500D0504 and S2000001D0505 through S2000100D0505. The recalled double seat Speedster Deuce Jogging strollers have model number: 20050216 and serial numbers: S3000001D0504 through S3000300D0504 and S3000001D0505 through S3000075D0505. Each stroller has a tag, located inside the child's seat compartment, which lists the model name and model number. A sticker on the rear frame lists the serial number.

CPSCAug 10, 2005Nationwide• Kelty Division of American Recreation Products Inc., of Boulder Colo.

Beckman Coulter Inc: Aqueduct Hematology Workflow Manager, software

Potentail for misidentification of historical patient results within the Aqueduct Hematology Workflow Manager software. In instances where the workflow manager software receives the same patient identifier for more than one patient the Aqueduct Workflow Manager software merges all results into one Patient File. The may cause test results to be associated with the wrong patient.

FDAAug 10, 2005AK, AZ, CA +15 more• Beckman Coulter Inc

Depuy Mitek, a Johnson & Johnson Co.: DePuy Mitek Straightshot Ligament Graft Passer/Protector,...

Mislabeled: The kit contained the incorrect Ligament Passer. The package contained a 9.5 mm instead of the labeled 11.5mm ligament passer

FDAAug 9, 2005CA, NC, VA• Depuy Mitek, a Johnson & Johnson Co.

Trek Diagnostic Systems: VersaTREK Myco AS.

Invitro diagnostic test kit used for testing to confirm the presence of tuberculosis contains interfering bioburden which can cause false positive results.

FDAAug 8, 2005AL, IL, IN +6 more• Trek Diagnostic Systems

Stryker Howmedica Osteonics Corp.: Reamer T-Handle; Non- Sterile; Howmedica Osteonics Corp.,...

Stryker Orthopaedics learned that the T-handles have the potential to not engage and not attach to the reamer properly.

FDAAug 8, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Navigation Reamer T-handle; Non Sterile; Howmedica Osteon...

Stryker Orthopaedics learned that the T-handles have the potential to not engage and not attach to the reamer properly.

FDAAug 8, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Biosense Webster, Inc.: Thermocool Irrigated Catheters Celsius LABEL US Part Num...

Increased complaints regarding catheters with leaks and flow obstruction.

FDAAug 8, 2005FL, IL, MA +3 more• Biosense Webster, Inc.

Guidant Endovascular Solutions, Inc.: Guidant OTW OMNILINK .018 & .035 Biliary Stent Systems

This action is being taken as a preventative measure as a result of an increased rate of complaints associated with stents becoming loose or dislodged from the delivery catheter.

FDAAug 8, 2005Nationwide• Guidant Endovascular Solutions, Inc.

Abbott Laboratories MPG: ABBOTT TestPack +Plus hCG Combo, list 3A60-16; the kit co...

False Positive results may be obtained with the identified lot of list 3A60-16 when using a negative patient sample or a negative control.

FDAAug 7, 2005IN• Abbott Laboratories MPG

Boston Scientific Scimed: Stainless Steel Greenfield Vena Cava Filter with 12 Fr. /...

Certain units within eleven lots of the 12 Fr Greenfield Vena Cava Filter may lack a taper on the braided sheath of the delivery system. The lack of a taper could lead to vessel damage as a result of the sheath catching on the edge of the vein and causing a tear.

FDAAug 5, 2005AL, AK, AZ +31 more• Boston Scientific Scimed

Datex Ohmeda, Inc. dba GE Healthcare: Ohmeda Giraffe SPOT PT Lite Phototherapy System

Phototherapy medical device may lose its position and can cause a safety hazard to the patient.

FDAAug 5, 2005IN• Datex Ohmeda, Inc. dba GE Healthcare

Boston Scientific Scimed: Titanium Greenfield Vena Cava Filter with 12 Fr./4,0 mm ...

FDAAug 5, 2005AL, AK, AZ +31 more• Boston Scientific Scimed

Stryker Instruments Div. of Stryker Corporation: Stryker brand Consolidated Operating Room Equipment (CORE...

Potential electrical shock hazard, in that the potential exists for the patient to be exposed to an earth-referenced electrical current.

FDAAug 5, 2005VA• Stryker Instruments Div. of Stryker Corporation